Status:
TERMINATED
A Prospective Randomized Postmarket Clinical Study of the TRANSITION Stabilization System
Lead Sponsor:
Globus Medical Inc
Conditions:
Acute Instabilities Thoracic, Lumbar and Sacral Spine
Chronic Instabilities Thoracic, Lumbar and Sacral Spine
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
This postmarket surveillance study is being conducted to evaluate the TRANSITION Stabilization System as an adjunct to fusion in the treatment of acute or chronic instabilities or deformities of the t...
Eligibility Criteria
Inclusion
- Any of the following acute or chronic instabilities or deformities of the thoracic, lumbar or sacral spine:
- degenerative spondylolisthesis with objective evidence of neurologic impairment,
- kyphosis, or
- pseudoarthrosis (failed previous fusion)
- Age 18 or older at the time of consent
- Able to understand and sign informed consent form
- Psychosocially, mentally and physically able to comply with protocol
- Able to meet the proposed follow-up schedule at 6 mo, 12 mo, and 24 mo
Exclusion
- Prior fusion surgery or another spinal device implanted in the thoracic, lumbar or sacral spine
- Requires treatment of more than two vertebral levels
- Lytic spondylolisthesis at the index level(s)
- Clinically compromised vertebral bodies at the affected level(s) due to current or past trauma
- Sustained pathologic fractures of the spine or hip, including prior fracture or trauma to vertebral structures at any thoracic, lumbar, or sacral level
- Morbid obesity defined as a body mass index \> 40, or a weight more than 100 lbs over ideal body weight
- Pregnant or interested in becoming pregnant within the next 2 years
- Active systemic or local infection
- Known allergy to device materials titanium, polycarbonate (PCU), polyethylene terepthalate (PET), or hydroxyapatite (HA).
- Taking medications or any drug known to potentially interfere with bone/soft tissue healing (e.g., steroids, excluding routine NSAIDs)
- Systemic disease including AIDS, HIV, Hepatitis C
- Has an active malignancy defined as a history of any invasive malignancy (except non-melanoma skin cancer), unless he/she has been treated with curative intent and there has been no clinical signs or symptoms of the malignancy for at least 5 years
- Neuromuscular disorders such as muscular dystrophy, spinal muscular atrophy, amyotrophic lateral sclerosis, etc.
- Participation in an investigational device or drug clinical trials within 30 days of surgery
- Acute mental illness or substance abuse
- Prisoners
Key Trial Info
Start Date :
April 19 2016
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 18 2017
Estimated Enrollment :
1 Patients enrolled
Trial Details
Trial ID
NCT02184520
Start Date
April 19 2016
End Date
May 18 2017
Last Update
March 15 2021
Active Locations (1)
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1
Fort Wayne Orthopaedics
Fort Wayne, Indiana, United States, 46804